Canonical Allele Identifier: CA395639625

Gene: HSD3B7

Linked Data

• dbSNP Id: rs1567370839
• gnomAD v2: 16-30997501-A-T
• gnomAD v4: 16-30986180-A-T
• MyVariant Identifiers: chr16:g.30997501A>T (hg19) ; chr16:g.30997501_30997505delinsTCCAT (hg19) ; chr16:g.30986180A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30986180A>T , CM000678.2:g.30986180A>T	GRCh38
NC_000016.9:g.30997501A>T , CM000678.1:g.30997501A>T	GRCh37
NC_000016.8:g.30905002A>T	NCBI36
NG_012346.1:g.5983A>T
NG_052948.1:g.33887A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297679.10:c.298A>T MANE Select	ENSP00000297679.5:p.Thr100Ser
ENST00000262520.10:c.298A>T	ENSP00000262520.6:p.Thr100Ser
ENST00000297679.9:c.298A>T	ENSP00000297679.5:p.Thr100Ser
ENST00000562932.5:c.421A>T	ENSP00000459852.1:p.Thr141Ser
ENST00000574447.1:c.298A>T	ENSP00000459689.1:p.Thr100Ser
NM_001142777.1:c.298A>T	NP_001136249.1:p.Thr100Ser
NM_001142778.1:c.298A>T	NP_001136250.1:p.Thr100Ser
NM_025193.3:c.298A>T	NP_079469.2:p.Thr100Ser
XM_005255601.3:c.298A>T	XP_005255658.2:p.Thr100Ser
XM_011545960.1:c.298A>T	XP_011544262.1:p.Thr100Ser
XM_011545961.1:c.298A>T	XP_011544263.1:p.Thr100Ser
XM_011545962.1:c.298A>T	XP_011544264.1:p.Thr100Ser
XM_011545960.2:c.298A>T	XP_011544262.1:p.Thr100Ser
XM_011545962.2:c.298A>T	XP_011544264.1:p.Thr100Ser
XM_017023732.1:c.298A>T	XP_016879221.1:p.Thr100Ser
NM_025193.4:c.298A>T MANE Select	NP_079469.2:p.Thr100Ser
NM_001142777.2:c.298A>T	NP_001136249.1:p.Thr100Ser
NM_001142778.2:c.298A>T	NP_001136250.1:p.Thr100Ser